AU2015254602B2 - Combination of a hyaluronic acid and of a sulphated polysaccharide - Google Patents
Combination of a hyaluronic acid and of a sulphated polysaccharide Download PDFInfo
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- AU2015254602B2 AU2015254602B2 AU2015254602A AU2015254602A AU2015254602B2 AU 2015254602 B2 AU2015254602 B2 AU 2015254602B2 AU 2015254602 A AU2015254602 A AU 2015254602A AU 2015254602 A AU2015254602 A AU 2015254602A AU 2015254602 B2 AU2015254602 B2 AU 2015254602B2
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- hyaluronic acid
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Abstract
The present invention relates to a combination comprising a hyaluronic acid or a salt thereof and a sulphated polysaccharide of which the molecular weight is between 5 and 25 kDa, which is of use in particular for combating the signs of skin ageing or for treating and healing skin wounds.
Description
COMBINATION OF A HYALURONIC ACID AND OF A SULPHATED POLYSACCHARIDE
FIELD OF THE INVENTION
The present invention relates to a novel combination of a hyaluronic acid or a salt thereof and of a low-molecular-weight sulphated polysaccharide; and to the use of said combination in the fields of anti-aging and healing.
PRIOR ART
Hyaluronic acid (HA) is a molecule with the most important role in the skin. It is indeed the principal component of the extracellular matrix. The latter refers to the set of extracellular macromolecules of the connective tissue. It is mainly made up of glycoproteins, pure proteins as well as glycosaminoglycans. HA is a linear non-sulphated glycosaminoglycan composed of repeating disaccharide units themselves composed of D-glucuronic acid and N-acetyl-D-glucosamine linked with alternating βΐ—3 and βΐ—4 glycosidic bonds between the dimers (Tammi R., Agren U.M., Tuhkanen A.L., Tammi M. Hyaluronan metabolism in skin. Progress in Histochemistry & Cytochemistry 29(2):1-81, 1994). In its native form, HA is a polymer having a very high molecular weight between 600,000 Da and 3 MDa (Toole BP. Hyaluronan: from extracellular glue to peracellular cue. Nat Rev Cancer 2004, 4:538-539).
With age, HA decreases in amount and in degree of polymerization, resulting in less water retained in the extracellular matrix. The skin then undergoes an aging process which leads to increased fibrosis and to a drop in elastic fiber content. During the aging process, a modification of skin structure and functions are observed. This aging is physiological in nature but can be also photoinduced, i.e. due to repeated exposure of the skin to sunlight, in particular ultraviolet light. The principal clinical signs of skin aging are the appearance of lines and deep wrinkles, which obviously increase with age. The furrows and wrinkles are marked; the skin becomes hollow and loses its firmness; on the surface, the skin loses its radiance.
Sulphated polysaccharides comprise, inter alia, sulphated fucans and sulphated ulvans having a molecular weight between 5 and 25 kDa.
These low-molecular-weight sulphated polysaccharides have advantageous biochemical properties: inhibition of degradation of collagen and elastin, restructuring, anti-inflammatory action, and induction of HA production.
During aging, fibroblasts enter senescence and their ability to proliferate greatly decreases. Thus, the fact of being able to stimulate the proliferation of these cells anew is one of the pathways studied for combating skin aging.
Furthermore, wound healing is a complex and dynamic biological process which brings into play the interaction of numerous local and systemic factors in normal tissue repair. Healing progresses in three interdependent phases: hemostasis and inflammation, proliferation and remodeling (General principles of wound healing. Witte MB, Barbul A. Surg Clin North Am. 1997 Jun; 77(3):509-28.). Proliferation involves three clearly observable processes: granulation, contraction and re-epithelialization.
During granulation, one observes the proliferation and migration toward the wound bed of cells which will intervene in the rest of the repair process. Thus, macrophages, fibroblasts and endothelial cells are found there. Macrophages constantly release chemotactic factors and growth factors. Fibroblasts construct the new cellular matrix necessary to cell growth at the base of the wound. This scaffolding supports cell migration. Lastly, endothelial cells trigger the formation of vascular buds which will constitute new capillaries, which will restore perfusion and ensure the supply of oxygen and of nutrients essential to the metabolic activity of cells in the wound.
Wound contraction is a mechanism of reducing wound size, and fibroblasts play a leading role in this contraction.
Re-epithelialization consists in the regeneration of an epidermis that covers a wound to form an effective barrier against the external environment, capable of becoming pigmented and of recovering its sensory and immune functions. It thus involves the cellular processes of keratinocyte migration and proliferation, but also the differentiation of this neo-epithelium and the restoration of a basal membrane that connects the dermis and the epidermis. When the migration of basal cells in the direction of the center of the wound enables the two wound edges to meet, a wave of
2015254602 06 Sep 2019 cell mitosis occurs to fill the spaces left by the migration and to provide cells for the epithelial tissue in three-dimensional regeneration.
The stages of proliferation of keratinocyte cells, fibroblasts or endothelial cells can be regarded as one of the functional phenomena showing the healing activity of an active agent.
Increased fibroblast proliferation would participate in the healing of a deep wound (reaching the dermis), whereas increased keratinocyte proliferation would participate in reepithelialization.
There remains a need to propose novel cosmetic compositions for combating the signs of skin aging.
The Applicant has shown the existence of synergy between hyaluronic acid and a lowmolecular-weight sulphated polysaccharide on fibroblast proliferation. This activity is particularly advantageous in the field of anti-aging but also in tissue regeneration and in healing skin lesions.
Where the terms comprise, comprises, comprised or comprising are used in this specification (including the claims) they are to be interpreted as specifying the presence of the stated features, integers, steps or components, but not precluding the presence of one or more other features, integers, steps or components, or group thereof.
DETAILED DESCRIPTION
The present invention provides a composition comprising a hyaluronic acid or a salt thereof having a weight average molecular weight between 60 and 120 EDa and a sulphated polysaccharide having a molecular weight between 5 and 25 kDa selected from sulphated fucans.
In the context of the present invention, the terms “hyaluronic acid”, “hyaluronic acid fragments”, “HA” and “hyaluronan” are used interchangeably to refer to hyaluronic acid. When hyaluronic acid is in salt form, it is referred to as hyaluronate.
In a particular embodiment of the invention, the combination comprises a hyaluronic acid or a salt thereof the weight average molecular weight (Mw) of which will be between 50,000 and 750,000 Da.
In a particular embodiment of the invention, the HA fragment or a salt thereof is characterized by a weight average molecular weight between 60 and 120 kDa, said molecular weight being measured by an analytical method combining size-exclusion chromatography (SEC) with a multi-angle light scattering photometer (MALS) coupled with a viscometer (VIS) and a differential refractometer (RI).
In a particular embodiment, it will be sodium hyaluronate.
The molecular weight of the HA or a salt thereof can be measured using the method of the European Pharmacopoeia which measures intrinsic viscosity with a Ubbelohde capillary viscometer (see European Pharmacopoeia 7.6, sodium hyaluronate monograph ref.: 01/2011:1472). This viscosity value is then related to average molecular weight by the Mark-Houwink relationship. This method is long and requires perfect reproducibility.
In the context of the present invention, the weight average molecular weight of the HA or a salt thereof is measured by the SEC-MALS-VIS-RI method, which is an analytical method combining size-exclusion chromatography (SEC) with a multi-angle light scattering photometer (MALS) coupled with a viscometer (VIS) and a differential refractometer. This technique makes it possible to obtain the weight average molecular weight (Mw).
This technique makes it possible to characterize the molecular weights of HAs in a precise and reproducible manner (Stepan Podzimek & al. Solution of Hyaluronic Acid and Comparison of SEC-MALS-VIS Data with Off-line Capillary Viscometry. Journal of Applied Polymer Science. 2009).
Coupling size-exclusion chromatography (SEC) with a MALS detector makes it possible, after injecting a polymer solution in a chromatographic system, to separate these polymers by size in the chromatographic column, to measure this size by light scattering and to quantify them using a differential refractometer or a UV spectrometer.
• Hyaluronic acid or a salt thereof is solubilized in aqueous 0.1 M NaCl solution then eluted on a column filled with polystyrene-divinylbenzene beads having a calibrated pore size. Large polymer chains do not pass into all the pores and are thus eluted before small chains.
• The MALS detector measures the scattering of incident light at various angles. These angles make it possible, by extrapolation, to measure Ro, which is the scattering at angle 0. Rq is directly proportional to molecule size.
• The Si response of the differential refractometer is proportional to the total mass Ci of the polymer having degree of polymerization z according to the following equation (1):
Si = K'dn/dcCi where: Si is thus the response of the differential refractometer,
K' is a constant linked to the apparatus, and
Ci is the total mass (weight) of the polymer having degree of polymerization z (Ci = Nj x Mj), Nj being the number of chains of molar mass Mj.
The refractive index increment dn/dc is in addition a specific value of the polymer under study.
This dn/dc ratio can be measured according to the following protocol exemplified with sodium hyaluronate.
a/ Apparatus and preparation of solutions:
Measurements are taken on a refractometer such as the Brice-Phoenix model having as incident light source a helium-neon laser (λ = 633 nm).
Various polymer concentrations to be studied are prepared independently by weighing (duration in solution = 24 hours). The respective refractive indices (dn) are then measured using the refractometer.
b/ Result
The results are presented in the form of a graph dn = ^concentration) (see Figure 1). A linear regression of type Y = A + B*X is then determined.
In the case of sodium hyaluronate, the values A and B determined are respectively A = -2.030 and B = 14927.911.
The dn/dc ratio thus corresponds to k x B where k is the constant of the apparatus which is equal to 0.97· 105 in this example.
For sodium hyaluronate, dn/dc is thus evaluated at 0.97-10 5 x 14927.911 = 0.145 ml/g.
The following formula gives the relationship between all the measured parameters:
Ro = K· Cr Mi where: Ro is the Rayleigh ratio at the scattering angle 0,
K is the constant of the apparatus,
Ci is the total mass of the polymer having degree of polymerization z [calculated according to equation (1)] of the injected solution, and Μ, is the molar mass of the polymer chain sought.
The weight average molecular weight Mw can then be calculated according to the formula:
Mw = ZCiMi/ZCi.
All the molecular weights are expressed in daltons.
Hyaluronic acid or a salt thereof, object of the present invention, can be obtained according to one of the processes known to persons skilled in the art, such as those mentioned in the document EP1987153.
HA is obtained mainly, in an industrial manner, by bacterial fermentation: hyaluronic acid filaments are synthesized by bacteria.
Thus in a particular embodiment of the invention, a native HA having a high molecular weight ranging generally from 1 MDa to 2 MDa is obtained by bacterial fermentation using a selected bacterial strain.
The polymer obtained can then be separated from the bacterium. The solution is then purified and then hydrolyzed by controlled acid hydrolysis until the desired molecular weight is obtained.
In the case of preparation of sodium hyaluronate, one will proceed to a neutralization step by adding NaOH.
The hyaluronic acid salt will preferentially be sodium hyaluronate.
In the context of the present invention, low-molecular-weight sulphated polysaccharides can be selected from sulphated fucans and sulphated ulvans having a molecular weight between 5 and 25 kDa.
Sulphated fucans are polysaccharides comprising sulphated L-fucose. These polysaccharides can be extracted in particular from brown algae, for example from the order Fucales or Laminariales.
Sulphated ulvans are sulphated anionic polysaccharides comprising uronic acids (e.g. glucuronic acid, iduronic acid) and sugars capable of being sulphated (e.g. 3-sulphate rhamnose, galactose, xylose, glucose) distributed in repeated motifs. The principal motifs are:
- ulvanobiuronic acid 3-sulphate type A consisting of 3-sulphate a-L-rhamnose linked with β-D-glucuronic acid by a 1—>4 type bond, and
- ulvanobiuronic acid 3-sulphate type B consisting of 3-sulphate a-L-rhamnose linked with α-L-iduronic acid by a 1—>4 type bond.
Ulvans can be extracted in particular from green algae of type ulva or enteromorpha (Ulva sp. and Enteromorpha sp.).
According to a particular embodiment, the low-molecular-weight sulphated fucan is as described in WO 2010/086197.
Mention may be made of the proprietary commercial product Ascophyscient® (Algues et Mer) extracted from the alga Ascophyllum nodosum.
According to another particular embodiment, the low-molecular-weight sulphated ulvan is as described in WO 2013/150253.
Mention may also be made of the fraction QT40® marketed by Green Tech based on a particular oligosaccharide from the alga Ulva lactuca: a sulpho-oligorhamnoglucuronan.
According to a particular embodiment of the invention, the mass ratio of hyaluronic acid to polysaccharide is between 0.1 and 10.
According to another particular embodiment of the invention, the mass ratio of hyaluronic acid to polysaccharide is between 0.5 and 5, and preferably between 0.5 and 2.
The present invention further relates to a combination of hyaluronic acid or a salt thereof and of a low-molecular-weight sulphated polysaccharide according to the invention (i.e. having a molecular weight between 5 and 25 kDa) for use to promote fibroblast proliferation.
The present invention also relates to a cosmetic composition comprising, as an anti-aging active ingredient, a combination of a hyaluronic acid or a salt thereof and of a sulphated polysaccharide having a molecular weight between 5 and 25 kDa and further comprising at least one cosmetically acceptable excipient.
Preferably, the cosmetically acceptable excipients are suited to topical administration.
Acceptable excipients make it possible in particular to ensure good stability and a pleasant texture and feel. They can also be, for example, formulation agents or additives of known and conventional use in cosmetics: mention may be made of surfactants, colorants, preservatives, fragrances, film-forming agents, thickeners, etc.
The anti-aging compositions can be in the forms commonly known for topical administration on the skin, i.e. in particular creams, emulsions, lotions, serums, masks, wrinkle fillers, eye liners, etc.
The object of the present invention is directed at the cosmetic use of the combination according to the present invention or of this cosmetic composition according to the invention for combating the signs of skin aging. The cosmetic use of the combination according to the present invention or the cosmetic composition according to the invention is more particularly intended to restore matter to the skin, to strengthen the firmness thereof and to visibly reduce marked wrinkles and deep furrows.
The present invention also relates to a method for combating the signs of skin aging comprising the administration, preferably topically, of an effective amount of a combination according to the invention or of a cosmetic composition according to the invention to a person in need thereof.
Another object of the present invention relates to a dermatological composition intended to accelerate skin repair in order to restore the integrity and the quality of the skin, comprising as dermatological or cosmetic active ingredient the combination of a hyaluronic acid or a salt thereof and of a sulphated polysaccharide the molecular weight of which is between 5 and 25 kDa mentioned above and further comprising at least one dermatologically or cosmetically acceptable excipient.
In a preferred embodiment of the invention, the composition is intended for topical application.
Dermatologically (pharmaceutically) or cosmetically compatible excipients can be any excipient among those known to persons skilled in the art for obtaining a composition for topical application in the form of a milk, a cream, a balm, an oil, a lotion, a gel, a foaming gel, an ointment, a spray, etc.
In a preferred embodiment, the composition will be in the form of a cream or an ointment.
In a particular embodiment, the dermatological and cosmetic compositions according to the invention comprise at least one other active ingredient.
This other active ingredient could in particular be selected from the group comprising anti-aging agents, healing agents, soothing agents, antipruritic agents, antioxidants, anti-radical agents, anti-UV agents, agents stimulating the synthesis of dermal macromolecules or energy metabolism, hydrating agents, depigmenting agents, antibacterials, antifungals, anti-inflammatories, or anesthetics.
According to a particular embodiment, the compositions according to the invention, preferably cosmetic, further comprise retinaldehyde. This supplementary anti-aging active agent is a direct precursor of retinoic acid for an immediate cellular metabolism reactivator effect. Retinaldehyde increases the expression of HA receptors, CD44, and induces HA synthesis.
The composition according to the invention then comprises a combination of hyaluronic acid or a salt thereof, of low-molecular-weight sulphated polysaccharide and of retinaldehyde. Such a combination has a restructuring and redensifying effect in the dermo-epidermal junction and the papillary dermis.
According to another embodiment of the invention, the composition will further comprise a tocopherol derivative including delta-tocopheryl-glucopyranoside: its powerful antioxidant effects protect the skin and preserve the radiance thereof.
The composition according to the invention then comprises a combination of hyaluronic acid or a salt thereof, of low-molecular-weight sulphated polysaccharide and of delta-tocopheryl-glucopyranoside.
According to another particular embodiment, the other active ingredient will be selected from healing agents, soothing agents and mixtures thereof. Such an active ingredient will be used preferably in dermatological compositions.
Lastly, another object of the present invention is directed at a combination of hyaluronic acid or a salt thereof and of low-molecular-weight sulphated polysaccharide or a dermatological composition containing same according to the invention for use as a medicine (more particularly a dermatological medicine), intended in particular for treating and healing skin lesions.
The present invention also relates to the use of a combination of a hyaluronic acid or a salt thereof and of a sulphated polysaccharide having a molecular weight between 5 and 25 kDa for the preparation of a medicine (more particularly a dermatological medicine), intended in particular for treating and healing skin lesions.
The present invention also relates to a method for treating and healing skin lesions comprising the administration, preferably topical, of an effective amount of a combination of a hyaluronic acid or a salt thereof and of a sulphated polysaccharide having a molecular weight between 5 and 25 kDa or a dermatological composition containing same according to the invention to a person in need thereof.
The dermatological and cosmetic compositions according to the invention are intended in particular for the care of skin injured:
• following invasive procedures/treatments: surgical procedures (exeresis, shaving) with or without suture, cryotherapy, laser ablation, moderate or heavy peeling, mesotherapy, curettage, • post-traumatically with superficial cuts or burns, • following superficial (noninvasive) procedures requiring a healing product which accelerates skin recovery, for long-term use (until complete repair of the skin), • following mild external damage: superficial abrasions, sunburn.
The treatment of lesions of the skin and the mucous membranes according to the invention may in particular comprise the treatment of cuts, sutures, abrasions, scratches, scrapes, scars following surgery or following an aesthetic dermatology procedure, superficial bums, sunburn.
The present invention further relates to the use of a cosmetic composition according to the invention intended to improve healing and skin repair.
The invention will be better understood upon reading the results below which illustrate the invention without limiting the scope thereof.
FIGURES
Figure 1 shows refractive index dn as a function of concentration c for sodium hyaluronate.
Figure 2 shows the effect of HA according to invention (HAF120) at 100 and 1000 pg/ml and of Ascophyscient® at 10 and 100 pg/ml on fibroblast proliferation. *: p < 0.05 and **: p < 0.01. Experiment representative of three independent experiments. Figure 3 shows the effect of HA according to invention (HAF120) at 100 pg/ml, Ascophyscient® at 10 pg/ml and a combination thereof on fibroblast proliferation. *: p < 0.05. Experiment representative of three independent experiments.
Figure 4 shows the effect of HA according to invention (HAF120) at 1000 pg/ml, Ascophyscient® at 10 pg/ml and a combination thereof on fibroblast proliferation. *: p < 0.05 and **: p < 0.01. Experiment representative of three independent experiments.
EXAMPLES
PHARMACOLOGICAL EVALUATION of the combination of a sodium hyaluronate fragment having a weight average molecular weight between 60 and 120 kPa (HAF120) and of a sulphated fucan having a low molecular weight (5-25 kPa) on fibroblast proliferation
Protocol:
The technique used is that of incorporation of a nucleotide, 5-bromo-2'-deoxyuridine (BrdU), a thymidine analog, in the PNA of S-phase cells, at 37°C. This technique makes it possible to quantify cells of which the advance in the cell cycle is characteristic of a proliferating cell (S-phase or PNA synthesis phase).
Normal human fibroblasts (NHF), isolated from surgical waste skin, are usually cultivated in Pulbecco’s modified Eagle’s medium (PMEM) with 10% fetal calf serum (FCS). In our experimental conditions, dilutions of the products to be tested are prepared in PMEM with 3% FCS.
The cells are first deprived of FCS for 24 hours to stop cell multiplication before incubating them in the presence of the molecules to be evaluated for 44 hours at 37°C, in a 5% CO2 atmosphere.
BrdU incorporation, proportional to cell proliferation rate, is evaluated by an anti-BrdU antibody system (Roche Applied Science). The corresponding absorbance (OP) is measured at 450 nm. This datum is thus proportional to cell proliferation rate.
The active agents evaluated are as follows:
- Positive control: epidermal growth factor (EGF) at 10 ng/ml
- Proprietary commercial product Ascophyscient® (Algues et Mer): 10 and 100 pg/ml (corresponding to 0.001% and 0.01%, respectively)
- 60-120 kPa sodium hyaluronate according to Example 1: 100 and 1000 pg/ml (corresponding to 0.01 and 0.1%, respectively)
- Combination comprising respectively Ascophyscient® and 60-120 kPa sodium hyaluronate at the following respective concentrations:
- 10 pg/ml + 100 pg/ml,
- 10 pg/ml + 1000 pg/ml.
Analysis of the results:
- expressed as OD (proportional to BrdU incorporation and thus to cell proliferation rate)
- expressed as percent stimulation:
OD treated [ _____________ x 100 ] - 100
OD control
- expressed as standard error of the mean: SEM = standard deviation (SD)A'n
Statistical analyses:
Statistical analyses using unpaired bilateral Student’s t-test were carried out on the raw OD values.
This test then gives p-values characterizing the significance of the results obtained for the various conditions. The degree of significance is established as follows:
significant for p < 0.05 (*) very significant for p < 0.01 (**) highly significant for p < 0.001 (***) not significant for p > 0.05
Results:
In these experimental conditions,
- Ascophyscient® induced fibroblast proliferation in a very reproducible and statistically significant manner, especially at 100 pg/ml (Figure 2).
- Sodium hyaluronate alone has a moderate effect on fibroblast proliferation (Figure 2).
- The combination of these two compounds induced fibroblast proliferation in a synergistic manner (Figures 3 and 4).
Conclusions:
In these experimental conditions, Ascophyscient® induced fibroblast proliferation in a very reproducible and statistically significant manner. The combination of Ascophyscient® with HAF120 induced fibroblast proliferation in a synergistic manner.
By inducing fibroblast proliferation, Ascophyscient® and the combination thereof with the 60-120 kDa sodium hyaluronate fragment restores cellular metabolism and participates in dermal repair and in combating aging.
EXEMPLARY COMPOSITIONS
Example 1:
| Name | Percentage |
| Purified water | q.s. 100% |
| Glycerin | 6 |
| Disodium EDTA | 0.1 |
| Phenoxyethanol | 0.35 |
| Acrylates/C 10-30 Alkyl Acrylate Crosspolymer (Carbopol® Ultrez 21) | 0.4 |
| Polyacrylate-13 & Polyisobutene & Polysorbate 20 & Water (Sepiplus™ 400) | 1 |
| Glyceryl Stearate & PEG-100 Stearate (Simulsol1M 165) | 4 |
| Cetyl Alcohol | 1 |
| Caprylic/Capric Triglycerides (Myritol® 318) | 10 |
| Dimethicone (DC 200) | 4 |
| Dicaprylyl Carbonate | 4 |
| 60-120 kDa Sodium hyaluronate according to the invention | 0.5 |
| Ascophyscient® | 0.3 |
| Fragrance | 0.1 |
Example 2:
| Name | Percentage |
| Purified water | q.s. 100% |
| Glycerin | 6 |
| Disodium EDTA | 0.1 |
| Phenoxyethanol | 0.35 |
| Acrylates/C 10-30 Alkyl Acrylate Crosspolymer (Carbopol® Ultrez 21) | 0.4 |
| Polyacrylate-13 & Polyisobutene & Polysorbate 20 & Water (Sepiplus™ 400) | 1 |
| Glyceryl Stearate & PEG-100 Stearate (Simulsol™ 165) | 4 |
| Cetyl alcohol | 1 |
| Caprylic/Capric Triglycerides (Myritol® 318) | 10 |
| Dimethicone (DC 200) | 4 |
| Isododecane | 4 |
| 60-120 kDa Sodium hyaluronate according to the invention | 0.5 |
| Ascophyscient® | 0.3 |
| Retinaldehyde | 0.05 |
| Fragrance | 0.1 |
Claims (14)
- The claims defining the invention are as follows:1. Composition comprising a hyaluronic acid or a salt thereof having a weight average molecular weight between 60 and 120 kDa and a sulphated polysaccharide having a5 molecular weight between 5 and 25 kDa selected from sulphated fiicans.
- 2. Composition according to claim 1, wherein the mass ratio of hyaluronic acid to polysaccharide is between 0.1 and 10.0
- 3. Use of a composition according to any one of claims 1 and 2, for the manufacture of a topical dermatological or cosmetic composition intended to promote fibroblast proliferation.
- 4. Topical use of a composition according to any one of claims 1 and 2, for combating the 5 signs of skin aging.
- 5. Use of a composition according to any one of claims 1 and 2, for the manufacture of a topical dermatological or cosmetic composition intended to treat skin lesions.0
- 6. Use of a composition according to any one of claims 1 and 2, for the manufacture of a topical dermatological or cosmetic composition intended to improve skin healing and repair.
- 7. A method for promoting fibroblast proliferation, combating the signs of skin aging, 25 treating skin lesions, or improving skin healing and repair comprising the topical administration to a person in need thereof of an effective amount of a composition according to any one of claims 1 and 2.
- 8. Dermatological or cosmetic composition comprising as active ingredient a composition 30 according to any one of claims 1 and 2, with at least one dermatologically or cosmetically acceptable excipient.
- 9 Composition according to claim 8, wherein it further comprises another active ingredient.
- 10. Composition according to claim 9, wherein the other active ingredient is selected from anti-aging agents, healing agents, soothing agents, antipruritic agents, anti-radical agents, anti-UV agents, agents stimulating the synthesis of dermal macromolecules or5 energy metabolism, hydrating agents, depigmenting agents, antibacterials, antifungals, anti-inflammatories, anesthetics and mixtures thereof.
- 11. Composition according to claim 9, wherein the other active ingredient is retinaldehyde.0
- 12. Composition according to claim 9, wherein the other active ingredient is deltatocopheryl-glucopyranoside.
- 13. Cosmetic use of the cosmetic composition according to any one of claims 8 to 12 for combating the signs of skin aging.
- 14. A method for combating the signs of skin aging comprising the administration to a person in need thereof of an effective amount of a cosmetic composition according to any one of claims 8 to 12.0 15. Use of a dermatological composition according to claim 8, for the manufacture of a medicine intended for the treatment of cuts, sutures, abrasions, scratches, scrapes, scars following surgery or following an aesthetic dermatology procedure, superficial burns, or sunburn.25 16. A method for treating cuts, sutures, abrasions, scratches, scrapes, scars following surgery or following an aesthetic dermatology procedure, superficial bums, or sunburn comprising the administration to a person in need thereof of an effective amount of a dermatological composition according to claim 8.
Applications Claiming Priority (3)
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|---|---|---|---|
| FR1453973A FR3020570B1 (en) | 2014-04-30 | 2014-04-30 | ASSOCIATION OF A HYALURONIC ACID AND A SULFATE POLYSACCHARIDE |
| FR1453973 | 2014-04-30 | ||
| PCT/EP2015/059544 WO2015166063A1 (en) | 2014-04-30 | 2015-04-30 | Combination of a hyaluronic acid and of a sulphated polysaccharide |
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| EP (1) | EP3137050B1 (en) |
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| CN106038355B (en) * | 2016-07-21 | 2019-11-12 | 中国科学院海洋研究所 | A kind of application of algal polysaccharides of high sulphation in Post-basking repairing mask |
| JPWO2019022250A1 (en) * | 2017-07-28 | 2020-07-09 | 国立大学法人九州大学 | Transdermal absorption composition with controlled release of water-soluble active ingredient |
| FR3075644B1 (en) * | 2017-12-27 | 2020-08-28 | Oreal | SULPHATED OLIGOSACCHARIDES AND THEIR COSMETIC USES |
| CN108553481B (en) * | 2018-05-25 | 2020-11-13 | 中国海洋大学 | Saccharide composition with wound healing promoting effect and application thereof |
| EP3829600A4 (en) * | 2018-07-27 | 2022-06-15 | Arc Medical Devices, Inc. | Low endotoxin fucan compositions, systems and methods |
| FR3098723B1 (en) * | 2019-07-18 | 2023-01-13 | Bionuclei | ECOBIOLOGICAL TREATMENT OF SIDE EFFECTS OF RADIOTHERAPY. |
| RU2753638C2 (en) * | 2020-01-24 | 2021-08-18 | ОБЩЕСТВО С ОГРАНИЧЕННОЙ ОТВЕТСТВЕННОСТЬЮ "НОВАСКИН" (ООО "Новаскин") | Gel composition for skin treatment |
| FR3113236A1 (en) * | 2020-08-05 | 2022-02-11 | Algues Et Mer | Purified fraction of fucoidans for the preparation of anti-aging cosmetic and/or dermatological compositions. |
| IT202000022477A1 (en) * | 2020-09-23 | 2022-03-23 | Sofar Swiss Sa | COMPOSITIONS INCLUDING A PLANT CHONDROITIN OR AN ANALOGUE THEREOF AND THEIR USE IN THE TREATMENT OF DISORDERS OF THE MUCOSA OF THE ORAL TRACT, PHARYNGO-LARYNGEAL AND/OR GASTRO-ESOPHAGEAL |
| CN115040535B (en) * | 2022-08-15 | 2022-12-16 | 华南理工大学 | Application of sulfated hyaluronic acid in preparing eye drops for preventing corneal fibrosis and corneal scar |
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| CN106255490B (en) | 2019-10-01 |
| JP6625558B2 (en) | 2019-12-25 |
| KR20160145788A (en) | 2016-12-20 |
| CA2946943C (en) | 2022-06-21 |
| EP3137050B1 (en) | 2020-03-04 |
| WO2015166063A1 (en) | 2015-11-05 |
| AU2015254602A1 (en) | 2016-12-22 |
| US9993417B2 (en) | 2018-06-12 |
| FR3020570A1 (en) | 2015-11-06 |
| CN106255490A (en) | 2016-12-21 |
| US20170049678A1 (en) | 2017-02-23 |
| JP2017514825A (en) | 2017-06-08 |
| BR112016024161B1 (en) | 2021-03-02 |
| RU2016146372A (en) | 2018-05-31 |
| CA2946943A1 (en) | 2015-11-05 |
| RU2016146372A3 (en) | 2018-10-03 |
| EP3137050A1 (en) | 2017-03-08 |
| MX2016014050A (en) | 2017-02-14 |
| BR112016024161A2 (en) | 2017-08-15 |
| FR3020570B1 (en) | 2017-07-21 |
| RU2683567C2 (en) | 2019-03-29 |
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